Behr ER - Search Results

1

Genotype-Phenotype Correlation of SCN5A Genotype in Patients With Brugada Syndrome and Arrhythmic Events: Insights From the SABRUS in 392 Probands.

Milman A, Behr ER, Gray B, Johnson DC, Andorin A, Hochstadt A, Gourraud JB, Maeda S, Takahashi Y, Jm Juang J, Kim SH, Kamakura T, Aiba T, Postema PG, Mizusawa Y, Denjoy I, Giustetto C, Conte G, Huang Z, Sarquella-Brugada G, Mazzanti A, Jespersen CH, Arbelo E, Brugada R, Calo L, Corrado D, Casado-Arroyo R, Allocca G, Takagi M, Delise P, Brugada J, Tfelt-Hansen J, Priori SG, Veltmann C, Yan GX, Brugada P, Gaita F, Leenhardt A, Wilde AAM, Kusano KF, Nam GB, Hirao K, Probst V, Belhassen B. Milman A, et al. Among authors: behr er. Circ Genom Precis Med. 2021 Oct;14(5):e003222. doi: 10.1161/CIRCGEN.120.003222. Epub 2021 Aug 31. Circ Genom Precis Med. 2021. PMID: 34461752 Clinical Trial.

2

New Insights Into the Genetic Basis of Inherited Arrhythmia Syndromes.

Gray B, Behr ER. Gray B, et al. Among authors: behr er. Circ Cardiovasc Genet. 2016 Dec;9(6):569-577. doi: 10.1161/CIRCGENETICS.116.001571. Circ Cardiovasc Genet. 2016. PMID: 27998945 Review. No abstract available.

3

Genotype-phenotype association in patients with SCN4A mutation - Authors' reply.

Matthews E, Männikkö R, Behr E, Hanna MG. Matthews E, et al. Lancet. 2019 Jun 8;393(10188):2301-2302. doi: 10.1016/S0140-6736(19)30214-4. Epub 2019 Jun 6. Lancet. 2019. PMID: 31180027 No abstract available.

4

J-Wave Syndromes, SCN5A, and Cardiac Conduction Reserve: Two Sides of the Same Coin?

Behr ER. Behr ER. J Am Coll Cardiol. 2021 Oct 19;78(16):1618-1620. doi: 10.1016/j.jacc.2021.09.003. J Am Coll Cardiol. 2021. PMID: 34649699 Free article. No abstract available.

5

The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome.

Makita N, Behr E, Shimizu W, Horie M, Sunami A, Crotti L, Schulze-Bahr E, Fukuhara S, Mochizuki N, Makiyama T, Itoh H, Christiansen M, McKeown P, Miyamoto K, Kamakura S, Tsutsui H, Schwartz PJ, George AL Jr, Roden DM. Makita N, et al. J Clin Invest. 2008 Jun;118(6):2219-29. doi: 10.1172/JCI34057. J Clin Invest. 2008. PMID: 18451998 Free PMC article.

6

The variation of the sarcolipin gene (SLN) in atrial fibrillation, long QT syndrome and sudden arrhythmic death syndrome.

Nyberg MT, Stoevring B, Behr ER, Ravn LS, McKenna WJ, Christiansen M. Nyberg MT, et al. Among authors: behr er. Clin Chim Acta. 2007 Jan;375(1-2):87-91. doi: 10.1016/j.cca.2006.06.020. Epub 2006 Jun 22. Clin Chim Acta. 2007. PMID: 17010328

7

Next generation diagnostics in inherited arrhythmia syndromes : a comparison of two approaches.

Ware JS, John S, Roberts AM, Buchan R, Gong S, Peters NS, Robinson DO, Lucassen A, Behr ER, Cook SA. Ware JS, et al. Among authors: behr er. J Cardiovasc Transl Res. 2013 Feb;6(1):94-103. doi: 10.1007/s12265-012-9401-8. Epub 2012 Sep 7. J Cardiovasc Transl Res. 2013. PMID: 22956155 Free PMC article.

8

National registry for sudden unexpected deaths of infants and children in England: why do we need one and do families want one?

Matthews E, Blair P, Sisodiya S, Jones S, Sebire N, Behr E, Fleming P. Matthews E, et al. Arch Dis Child. 2019 Oct;104(10):989-993. doi: 10.1136/archdischild-2018-316542. Epub 2019 Apr 20. Arch Dis Child. 2019. PMID: 31005897 Free PMC article.

9

Functional assessment of compound mutations in the KCNQ1 and KCNH2 genes associated with long QT syndrome.

Grunnet M, Behr ER, Calloe K, Hofman-Bang J, Till J, Christiansen M, McKenna WJ, Olesen SP, Schmitt N. Grunnet M, et al. Among authors: behr er. Heart Rhythm. 2005 Nov;2(11):1238-49. doi: 10.1016/j.hrthm.2005.07.025. Heart Rhythm. 2005. PMID: 16253915

10

Prolongation of the QT interval and post-extrasystolic augmentation of the TU-wave during emotional stress.

Batchvarov VN, Bajpai A, Behr E. Batchvarov VN, et al. Indian Pacing Electrophysiol J. 2008 Apr 1;8(2):146-8. Indian Pacing Electrophysiol J. 2008. PMID: 18379661 Free PMC article.

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